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Functional Outcome in Patients That Underwent Laparoscopic Sigmoid and/or Rectum Resection

To Assess the Functional Outcome in Patients That Underwent Laparoscopic Sigmoid and/or Rectum Resection

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01953250
Enrollment
143
Registered
2013-09-30
Start date
2012-06-30
Completion date
2013-06-30
Last updated
2013-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis

Keywords

Deep infiltrating endometriosis, Laparoscopic sigmoid resection, laparoscopic rectum resection, Colorectal surgery

Brief summary

Questionnaire To assess the functional outcome in patients that underwent laparoscopic sigmoid and/or rectum resection.

Detailed description

A questionnaire will be sent to every patient by mail. The questionnaire that will be used is the COREFO questionnaire (ColoRectal Functional Outcome). Depending on the amount of responses, we will try to make connections between peri-operative data and functional outcome after considerable period of follow-up. Peri-operative factors include grade of endometriosis, surgical technique and post-operative complications.

Interventions

None listed

Sponsors

Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Patients that underwent laparoscopic sigmoid and/or rectum resection with the indication of deep infiltrating endometriosis

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
ColoRectal Functional Outcome1 dayOperation: between 1997 and 2011 Questionnaire to assess the colorectal function sent once in 2012

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026